Does MiRNA gene expression predict gastric cancer stage and localization?

Autor: Selami Ilgaz Kayilioglu, Ahmet Korkut Belli, Önder Özcan, Özgür İlhan Çelik, Murat Polat, Murat Kara, Mehmet Kaplan
Přispěvatelé:
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Mikrobiyoloji
Angiogenesis
Cellular differentiation
Tıbbi Laboratuar Teknolojisi
lcsh:Medicine
Nörolojik Bilimler
Radyoloji
Nükleer Tıp
Tıbbi Görüntüleme

Transplantasyon
Medicine
Anatomi ve Morfoloji
Sağlık Bilimleri ve Hizmetleri
Enfeksiyon Hastalıkları
Patoloji
Dermatoloji
Cerrahi
lcsh:R5-920
Alerji
Odyoloji ve Konuşma-Dil Patolojisi
Hücre Biyolojisi
Tıbbi İnformatik
Kadın Hastalıkları ve Doğum
Onkoloji
Periferik Damar Hastalıkları
Psikiyatri
Tropik Tıp
Gastroenteroloji ve Hepatoloji
Romatoloji
MiRNA
lcsh:Medicine (General)
Biyoloji
Temel Sağlık Hizmetleri
Biyoteknoloji ve Uygulamalı Mikrobiyoloji
Kalp ve Kalp Damar Sistemi
Endokrinoloji ve Metabolizma
Anestezi
Biyofizik
Klinik Nöroloji
Üroloji ve Nefroloji
Solunum Sistemi
Acil Tıp
Androloji
microRNA
expression
Spor Bilimleri
Kulak
Burun
Boğaz

Halk ve Çevre Sağlığı
gastric carcinoma
gene
Geriatri ve Gerontoloji
Genel ve Dahili Tıp
Gene
Tumor marker
Fizyoloji
Göz Hastalıkları
İmmünoloji
business.industry
Cell growth
lcsh:R
Cancer
Tıbbi Araştırmalar Deneysel
medicine.disease
Tıbbi Etik
Stem cell division
Adli Tıp
Pediatri
Ortopedi
Hematoloji
Tamamlayıcı ve Entegre Tıp
Rehabilitasyon
Cancer research
Biyokimya ve Moleküler Biyoloji
Yoğun Bakım
Tıp

business
Zdroj: Medicine Science, Vol 8, Iss 1, Pp 255-9 (2019)
ISSN: 2147-0634
Popis: Gastric cancer comprises 10% of all cancers in the world and is rarely seen before the age of 30. Different genetic interactions or molecular changes like e-cadherin, P16, APC, c-erb B2, c-met, ras, or c-myc have been described in the pathogenesis of the disease. MiRNAs play critical roles in various biological processes such as cell proliferation, cell differentiation, apoptosis, repairing of DNA damage, angiogenesis, stress response, and stem cell division. The aim of this study is to investigate the relationship between miRNA gene expressions and gastric cancer. Method: Sixty-four patients with gastric cancer diagnosed consecutively in our pathology laboratory and 30 consecutive participants with normal gastric tissue, as a control group, were included in our study between 2011 and 2013. Total miRNAs were obtained by using genomic miRNA extraction kit (QIAGEN Sample & Assay Technologies, Hilden, Germany) after the samples had been deparaffinized. MiR-21, 107, 141, 150, 192, 202, 218, 331 gene expressions were evaluated by using real time-PCR (RT-PCR) from the whole miRNA. Results: MiR-331 was downregulated in the stage 2 patients and the rest of the miRNAs were significantly upregulated (p < 0.001). All miRNAs were significantly upregulated in the stage 3a patients (p < 0.001). In the antrum localized tumors, miR-107, -150, -202, -218, and -331 were significantly upregulated, whereas miR-21, -192 were statistically downregulated (p < 0.05). In the cardia localized tumors, miR-21 (p > 0.05) was downregulated and miR-107, -150, -202, -218, and -331 were upregulated (p < 0.05) Different gene expressions of miRNAs according to the different localizations of gastric cancer and different stages suggest that it can be tumor marker to predict the stage and localization of gastric cancer. [Med-Science 2019; 8(1.000): 255-9]
Databáze: OpenAIRE